Drug Facts

Active ingredient (per capsulle)

Sennosides 8.3mg

Stimulant Laxative

Choking: Taking this product without adequate fluid may cause it to swell and block your throat or esophagus and may cause choking. Do not take this product if you have difficulty in swallowing. If you experience chest pain. vomiting or difficulty in swallowing or breathing after taking this product seek immediate medical attention

• stomach pain • nausea • vomiting • noticed a sudden change in bowel habits that continues for a period of 2 weeks.

• you have rectal bleeding • you fail to have bowel movement after use of a laxative. These may indicale a serious condition

• ask a health professional before use

In case of overdose get medical help or contact a Poison Control Center right away

take this product with a full glass (8oz) of water or other liquid. Taking this product without enough liquid may cause choking. (See choking warning.)


adults and children 12 years of age and older:	2 capsules 2 times daily
children 6 to under 12 years of age:	1 capsule once or twice daily
children under 6 years of age:	consult a doctor

• store below 86°F (30°C)

fennel seed powder, gelatin, lactobacillus acidophilus powder, papaya leaf powder, psyllium husk powder, rose hips fruit powder

1-800-822-6225

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SUPER COLON CLEANSE
sennosides capsule

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX)	SENNOSIDES	8.3 mg

Ingredient Name	Strength
Inactive Ingredients
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:57348-897-60	1 in 1 CARTON	09/16/2018	04/30/2026
1		60 in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC:57348-897-10	1 in 1 CARTON	09/16/2018	04/30/2026
2		100 in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC:57348-897-12	1 in 1 CARTON	09/16/2018	04/30/2026
3		120 in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC:57348-897-24	1 in 1 CARTON	09/16/2018	04/30/2026
4		240 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	09/16/2018	04/30/2026

Labeler - Health Plus Inc. (131279275)

Registrant - Health Plus Inc. (131279275)

Name	Address	ID/FEI	Business Operations
Establishment
Health Plus Inc.		131279275	manufacture(57348-897)